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Three dimensional structure of broadly neutralizing anti - hepatitis C virus (HCV) glycoprotein E2 single chain fv fragment 1:7

Analyse Three dimensional structure of broadly neutralizing anti - hepatitis C virus… in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
3U6R
Type
protein
Length
463 residues
Chains
4
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Antibody 1:7 (heavy chain); Antibody 1:7 (light chain)
Ligands
SO4
Pockets
6 · best druggability 0.76

Structure

x-ray diffraction · 3 distinct chains · 4% helix, 51% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
HAntibody 1:7 (heavy chain)protein1265% helix, 52% strand—
L, BAntibody 1:7 (light chain)protein1053% helix, 52% strand—
AAntibody 1:7 (heavy chain)protein1275% helix, 50% strand—

Ligands and binding sites

  • SO4 · Sulfate ion · ion · chains H, L

Binding sites are the residues within 4.5 Å of a ligand's heavy atoms.

Pockets

6 pockets found on a 1 Å grid, 3 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
18970.760.7966empty
23530.580.7632empty
32920.560.7628empty
4900.340.7415empty
5550.280.7512empty

Interfaces

5 interfaces between chains.

  • H–L · 931 Ų buried · 17 hydrogen bonds · protein-protein
  • A–B · 823 Ų buried · 11 hydrogen bonds · protein-protein
  • H–B · 339 Ų buried · 4 hydrogen bonds · protein-protein
  • L–A · 326 Ų buried · 2 hydrogen bonds · protein-protein
  • L–B · 93 Ų buried · 1 hydrogen bond · protein-protein

Modifications

Observed in the structure: 4 disulfide (disulfide).

Compared structures

  • 3U6R · Three dimensional structure of broadly neutralizing anti - Hepatitis C virus (HCV)… · the same entry in another collection · chain A against A, TM-score 1.00

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